FDA 510(k) Applications Submitted by PRECISE MEDICAL PRODUCTS, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061409 | 05/22/2006 | SMARTINFUSER PAINPUMP, MODEL P49220 W/CATHETER SET; P49224N W/O CATHETER SET | PRECISE MEDICAL PRODUCTS, LTD. |
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